CA2722770C - Antisapstain compositions comprising a haloalkynyl compound, an azole and an unsaturated acid - Google Patents

Antisapstain compositions comprising a haloalkynyl compound, an azole and an unsaturated acid Download PDF

Info

Publication number: CA2722770C
Authority: CA; Canada
Prior art keywords: acid; composition; metal salt; formulation; ipbc
Prior art date: 2008-04-30
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Fee Related

Application number

CA 2722770

Other languages

English (en)

French (fr)

Other versions

CA2722770A1 (en

Inventor

Paul Stuart Warburton

Lee Mason

Andrew Stewart Hughes

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Arch Timber Protection Ltd

Original Assignee

Arch Timber Protection Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2008-04-30

Filing date

2009-04-30

Publication date

2015-02-17

2009-04-30 Application filed by Arch Timber Protection Ltd filed Critical Arch Timber Protection Ltd

2009-11-05 Publication of CA2722770A1 publication Critical patent/CA2722770A1/en

2015-02-17 Application granted granted Critical

2015-02-17 Publication of CA2722770C publication Critical patent/CA2722770C/en

Status Expired - Fee Related legal-status Critical Current

2029-04-30 Anticipated expiration legal-status Critical

Links

239000000203 mixture Substances 0.000 title claims abstract description 224
-1 haloalkynyl compound Chemical class 0.000 title claims abstract description 86
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 title claims abstract description 40
239000002253 acid Substances 0.000 title claims description 60
239000002023 wood Substances 0.000 claims abstract description 51
239000000758 substrate Substances 0.000 claims abstract description 35
150000001732 carboxylic acid derivatives Chemical class 0.000 claims abstract description 15
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 claims abstract description 14
238000000034 method Methods 0.000 claims abstract description 12
238000009472 formulation Methods 0.000 claims description 136
229940099451 3-iodo-2-propynylbutylcarbamate Drugs 0.000 claims description 101
WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-UHFFFAOYSA-N 0.000 claims description 101
239000005822 Propiconazole Substances 0.000 claims description 49
STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 claims description 49
RSWGJHLUYNHPMX-UHFFFAOYSA-N 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid Chemical compound C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 37
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 37
WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 claims description 29
235000010234 sodium benzoate Nutrition 0.000 claims description 29
239000004299 sodium benzoate Substances 0.000 claims description 29
150000003839 salts Chemical class 0.000 claims description 25
BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 claims description 22
BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 claims description 22
PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 claims description 21
239000005839 Tebuconazole Substances 0.000 claims description 21
150000001875 compounds Chemical class 0.000 claims description 21
239000011734 sodium Substances 0.000 claims description 20
WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 claims description 19
229910052783 alkali metal Inorganic materials 0.000 claims description 19
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 16
125000004432 carbon atom Chemical group C* 0.000 claims description 15
BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 claims description 12
239000000463 material Substances 0.000 claims description 12
235000010199 sorbic acid Nutrition 0.000 claims description 12
239000004334 sorbic acid Substances 0.000 claims description 12
229940075582 sorbic acid Drugs 0.000 claims description 12
125000000217 alkyl group Chemical group 0.000 claims description 11
125000003118 aryl group Chemical group 0.000 claims description 11
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 10
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 10
ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 claims description 10
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 10
229910052708 sodium Inorganic materials 0.000 claims description 10
PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 claims description 9
239000005795 Imazalil Substances 0.000 claims description 9
239000000839 emulsion Substances 0.000 claims description 9
229960002125 enilconazole Drugs 0.000 claims description 9
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 8
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 8
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 7
CHHHXKFHOYLYRE-UHFFFAOYSA-M 2,4-Hexadienoic acid, potassium salt (1:1), (2E,4E)- Chemical compound [K+].CC=CC=CC([O-])=O CHHHXKFHOYLYRE-UHFFFAOYSA-M 0.000 claims description 7
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 7
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 7
239000005642 Oleic acid Substances 0.000 claims description 7
229910052739 hydrogen Inorganic materials 0.000 claims description 7
239000007788 liquid Substances 0.000 claims description 7
235000010241 potassium sorbate Nutrition 0.000 claims description 7
239000004302 potassium sorbate Substances 0.000 claims description 7
229940069338 potassium sorbate Drugs 0.000 claims description 7
YWWVWXASSLXJHU-AATRIKPKSA-N (9E)-tetradecenoic acid Chemical compound CCCC\C=C\CCCCCCCC(O)=O YWWVWXASSLXJHU-AATRIKPKSA-N 0.000 claims description 6
239000005711 Benzoic acid Substances 0.000 claims description 6
235000010233 benzoic acid Nutrition 0.000 claims description 6
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 6
STMIIPIFODONDC-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(O)(CCCC)CN1C=NC=N1 STMIIPIFODONDC-UHFFFAOYSA-N 0.000 claims description 5
UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 claims description 5
NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 claims description 5
239000005757 Cyproconazole Substances 0.000 claims description 5
229910052736 halogen Inorganic materials 0.000 claims description 5
150000002367 halogens Chemical class 0.000 claims description 5
239000001257 hydrogen Substances 0.000 claims description 5
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 5
229910052700 potassium Inorganic materials 0.000 claims description 5
MHVJRKBZMUDEEV-UHFFFAOYSA-N (-)-ent-pimara-8(14),15-dien-19-oic acid Natural products C1CCC(C(O)=O)(C)C2C1(C)C1CCC(C=C)(C)C=C1CC2 MHVJRKBZMUDEEV-UHFFFAOYSA-N 0.000 claims description 4
239000004283 Sodium sorbate Substances 0.000 claims description 4
YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 claims description 4
AKNQMEBLVAMSNZ-UHFFFAOYSA-N azaconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCCO1 AKNQMEBLVAMSNZ-UHFFFAOYSA-N 0.000 claims description 4
229950000294 azaconazole Drugs 0.000 claims description 4
239000001530 fumaric acid Substances 0.000 claims description 4
125000001624 naphthyl group Chemical group 0.000 claims description 4
SECPZKHBENQXJG-FPLPWBNLSA-N palmitoleic acid Chemical compound CCCCCC\C=C/CCCCCCCC(O)=O SECPZKHBENQXJG-FPLPWBNLSA-N 0.000 claims description 4
LROWVYNUWKVTCU-STWYSWDKSA-M sodium sorbate Chemical compound [Na+].C\C=C\C=C\C([O-])=O LROWVYNUWKVTCU-STWYSWDKSA-M 0.000 claims description 4
235000019250 sodium sorbate Nutrition 0.000 claims description 4
MHVJRKBZMUDEEV-APQLOABGSA-N (+)-Pimaric acid Chemical compound [C@H]1([C@](CCC2)(C)C(O)=O)[C@@]2(C)[C@H]2CC[C@](C=C)(C)C=C2CC1 MHVJRKBZMUDEEV-APQLOABGSA-N 0.000 claims description 3
YNWVFADWVLCOPU-MDWZMJQESA-N (1E)-1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol Chemical compound C1=NC=NN1/C(C(O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1 YNWVFADWVLCOPU-MDWZMJQESA-N 0.000 claims description 3
ZMYFCFLJBGAQRS-IAGOWNOFSA-N (2S,3R)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@]1(CN2N=CN=C2)[C@@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IAGOWNOFSA-N 0.000 claims description 3
OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 claims description 3
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 3
JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 claims description 3
VGPIBGGRCVEHQZ-UHFFFAOYSA-N 1-(biphenyl-4-yloxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC(C=C1)=CC=C1C1=CC=CC=C1 VGPIBGGRCVEHQZ-UHFFFAOYSA-N 0.000 claims description 3
LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 claims description 3
WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 claims description 3
ZOMKCDYJHAQMCU-UHFFFAOYSA-N 4-butyl-1,2,4-triazole Chemical compound CCCCN1C=NN=C1 ZOMKCDYJHAQMCU-UHFFFAOYSA-N 0.000 claims description 3
YWWVWXASSLXJHU-UHFFFAOYSA-N 9E-tetradecenoic acid Natural products CCCCC=CCCCCCCCC(O)=O YWWVWXASSLXJHU-UHFFFAOYSA-N 0.000 claims description 3
239000005760 Difenoconazole Substances 0.000 claims description 3
239000005785 Fluquinconazole Substances 0.000 claims description 3
239000005787 Flutriafol Substances 0.000 claims description 3
239000005813 Penconazole Substances 0.000 claims description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 3
239000005840 Tetraconazole Substances 0.000 claims description 3
239000005846 Triadimenol Substances 0.000 claims description 3
125000002877 alkyl aryl group Chemical group 0.000 claims description 3
125000003710 aryl alkyl group Chemical group 0.000 claims description 3
125000000753 cycloalkyl group Chemical group 0.000 claims description 3
BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 claims description 3
FBOUIAKEJMZPQG-BLXFFLACSA-N diniconazole-M Chemical compound C1=NC=NN1/C([C@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-BLXFFLACSA-N 0.000 claims description 3
IJJVMEJXYNJXOJ-UHFFFAOYSA-N fluquinconazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1N1C(=O)C2=CC(F)=CC=C2N=C1N1C=NC=N1 IJJVMEJXYNJXOJ-UHFFFAOYSA-N 0.000 claims description 3
FQKUGOMFVDPBIZ-UHFFFAOYSA-N flusilazole Chemical compound C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 FQKUGOMFVDPBIZ-UHFFFAOYSA-N 0.000 claims description 3
125000001424 substituent group Chemical group 0.000 claims description 3
BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 claims description 3
HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims description 2
235000021319 Palmitoleic acid Nutrition 0.000 claims description 2
JAZBEHYOTPTENJ-JLNKQSITSA-N all-cis-5,8,11,14,17-icosapentaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O JAZBEHYOTPTENJ-JLNKQSITSA-N 0.000 claims description 2
MBMBGCFOFBJSGT-KUBAVDMBSA-N all-cis-docosa-4,7,10,13,16,19-hexaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC(O)=O MBMBGCFOFBJSGT-KUBAVDMBSA-N 0.000 claims description 2
229940114079 arachidonic acid Drugs 0.000 claims description 2
235000021342 arachidonic acid Nutrition 0.000 claims description 2
SECPZKHBENQXJG-UHFFFAOYSA-N cis-palmitoleic acid Natural products CCCCCCC=CCCCCCCCC(O)=O SECPZKHBENQXJG-UHFFFAOYSA-N 0.000 claims description 2
125000000392 cycloalkenyl group Chemical group 0.000 claims description 2
229960005135 eicosapentaenoic acid Drugs 0.000 claims description 2
JAZBEHYOTPTENJ-UHFFFAOYSA-N eicosapentaenoic acid Natural products CCC=CCC=CCC=CCC=CCC=CCCCC(O)=O JAZBEHYOTPTENJ-UHFFFAOYSA-N 0.000 claims description 2
235000020673 eicosapentaenoic acid Nutrition 0.000 claims description 2
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
239000011976 maleic acid Substances 0.000 claims description 2
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 2
WXVXYGWYSRYKKS-UHFFFAOYSA-N methyl n-(1h-benzimidazol-2-yl)carbamate;n-propyl-n-[2-(2,4,6-trichlorophenoxy)ethyl]imidazole-1-carboxamide Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1.C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl WXVXYGWYSRYKKS-UHFFFAOYSA-N 0.000 claims description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
ITCAUAYQCALGGV-XTICBAGASA-M sodium;(1r,4ar,4br,10ar)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate Chemical compound [Na+].C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C([O-])=O ITCAUAYQCALGGV-XTICBAGASA-M 0.000 claims description 2
239000004308 thiabendazole Substances 0.000 claims description 2
235000010296 thiabendazole Nutrition 0.000 claims description 2
229960004546 thiabendazole Drugs 0.000 claims description 2
WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical group S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 claims description 2
125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims 1
HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 claims 1
DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 claims 1
230000000694 effects Effects 0.000 abstract description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 74
WGYZMNBUZFHYRX-UHFFFAOYSA-N 1-(1-methoxypropan-2-yloxy)propan-2-ol Chemical compound COCC(C)OCC(C)O WGYZMNBUZFHYRX-UHFFFAOYSA-N 0.000 description 55
239000004094 surface-active agent Substances 0.000 description 53
230000000052 comparative effect Effects 0.000 description 38
150000007513 acids Chemical class 0.000 description 23
229940050390 benzoate Drugs 0.000 description 21
239000002904 solvent Substances 0.000 description 21
239000002243 precursor Substances 0.000 description 16
239000004359 castor oil Substances 0.000 description 15
235000019438 castor oil Nutrition 0.000 description 15
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 15
KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 13
150000001412 amines Chemical class 0.000 description 13
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 13
229920005989 resin Polymers 0.000 description 13
239000011347 resin Substances 0.000 description 13
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 13
150000001735 carboxylic acids Chemical class 0.000 description 8
125000000524 functional group Chemical group 0.000 description 8
239000000417 fungicide Substances 0.000 description 8
RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 description 7
150000002148 esters Chemical class 0.000 description 7
239000004615 ingredient Substances 0.000 description 7
235000021313 oleic acid Nutrition 0.000 description 7
150000003856 quaternary ammonium compounds Chemical class 0.000 description 7
150000004671 saturated fatty acids Chemical class 0.000 description 7
235000008331 Pinus X rigitaeda Nutrition 0.000 description 6
235000011613 Pinus brutia Nutrition 0.000 description 6
241000018646 Pinus brutia Species 0.000 description 6
239000000654 additive Substances 0.000 description 6
229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 6
238000005253 cladding Methods 0.000 description 6
125000004122 cyclic group Chemical group 0.000 description 6
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 6
125000001072 heteroaryl group Chemical group 0.000 description 6
229920006395 saturated elastomer Polymers 0.000 description 6
239000003784 tall oil Substances 0.000 description 6
229920002413 Polyhexanide Polymers 0.000 description 5
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OMFRMAHOUUJSGP-IRHGGOMRSA-N bifenthrin Chemical compound C1=CC=C(C=2C=CC=CC=2)C(C)=C1COC(=O)[C@@H]1[C@H](\C=C(/Cl)C(F)(F)F)C1(C)C OMFRMAHOUUJSGP-IRHGGOMRSA-N 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
150000001642 boronic acid derivatives Chemical class 0.000 description 1
238000005282 brightening Methods 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
230000001680 brushing effect Effects 0.000 description 1
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
FAOSYNUKPVJLNZ-UHFFFAOYSA-N butylstannane Chemical compound CCCC[SnH3] FAOSYNUKPVJLNZ-UHFFFAOYSA-N 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
150000003857 carboxamides Chemical class 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000007942 carboxylates Chemical class 0.000 description 1
YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 description 1
229960001927 cetylpyridinium chloride Drugs 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
CWFOCCVIPCEQCK-UHFFFAOYSA-N chlorfenapyr Chemical compound BrC1=C(C(F)(F)F)N(COCC)C(C=2C=CC(Cl)=CC=2)=C1C#N CWFOCCVIPCEQCK-UHFFFAOYSA-N 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
125000000068 chlorophenyl group Chemical group 0.000 description 1
SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000003240 coconut oil Substances 0.000 description 1
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239000003026 cod liver oil Substances 0.000 description 1
235000012716 cod liver oil Nutrition 0.000 description 1
238000010276 construction Methods 0.000 description 1
239000013068 control sample Substances 0.000 description 1
SBFUAYPDMPMYBP-ATMONBRVSA-L copper (Z)-cyclohexyl-oxido-oxidoiminoazanium Chemical compound [Cu++].[O-]\N=[N+](/[O-])C1CCCCC1.[O-]\N=[N+](/[O-])C1CCCCC1 SBFUAYPDMPMYBP-ATMONBRVSA-L 0.000 description 1
229940116318 copper carbonate Drugs 0.000 description 1
229910001956 copper hydroxide Inorganic materials 0.000 description 1
229940120693 copper naphthenate Drugs 0.000 description 1
SEVNKWFHTNVOLD-UHFFFAOYSA-L copper;3-(4-ethylcyclohexyl)propanoate;3-(3-ethylcyclopentyl)propanoate Chemical compound [Cu+2].CCC1CCC(CCC([O-])=O)C1.CCC1CCC(CCC([O-])=O)CC1 SEVNKWFHTNVOLD-UHFFFAOYSA-L 0.000 description 1
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AEJIMXVJZFYIHN-UHFFFAOYSA-N copper;dihydrate Chemical compound O.O.[Cu] AEJIMXVJZFYIHN-UHFFFAOYSA-N 0.000 description 1
235000005687 corn oil Nutrition 0.000 description 1
239000002285 corn oil Substances 0.000 description 1
239000003431 cross linking reagent Substances 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
229960001591 cyfluthrin Drugs 0.000 description 1
QQODLKZGRKWIFG-QSFXBCCZSA-N cyfluthrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@@H](C#N)C1=CC=C(F)C(OC=2C=CC=CC=2)=C1 QQODLKZGRKWIFG-QSFXBCCZSA-N 0.000 description 1
229960005424 cypermethrin Drugs 0.000 description 1
KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 description 1
QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 description 1
229960002483 decamethrin Drugs 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
SCXCDVTWABNWLW-UHFFFAOYSA-M decyl-dimethyl-octylazanium;chloride Chemical compound [Cl-].CCCCCCCCCC[N+](C)(C)CCCCCCCC SCXCDVTWABNWLW-UHFFFAOYSA-M 0.000 description 1
NFWKVWVWBFBAOV-MISYRCLQSA-N dehydroabietic acid Chemical compound OC(=O)[C@]1(C)CCC[C@]2(C)C3=CC=C(C(C)C)C=C3CC[C@H]21 NFWKVWVWBFBAOV-MISYRCLQSA-N 0.000 description 1
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150000001991 dicarboxylic acids Chemical class 0.000 description 1
WURGXGVFSMYFCG-UHFFFAOYSA-N dichlofluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=CC=C1 WURGXGVFSMYFCG-UHFFFAOYSA-N 0.000 description 1
MVTVVKOMNZGDGD-UHFFFAOYSA-M didecyl(dimethyl)azanium;hydron;carbonate Chemical compound OC([O-])=O.CCCCCCCCCC[N+](C)(C)CCCCCCCCCC MVTVVKOMNZGDGD-UHFFFAOYSA-M 0.000 description 1
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239000003995 emulsifying agent Substances 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
210000002919 epithelial cell Anatomy 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
229940116333 ethyl lactate Drugs 0.000 description 1
YREQHYQNNWYQCJ-UHFFFAOYSA-N etofenprox Chemical compound C1=CC(OCC)=CC=C1C(C)(C)COCC1=CC=CC(OC=2C=CC=CC=2)=C1 YREQHYQNNWYQCJ-UHFFFAOYSA-N 0.000 description 1
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HJUFTIJOISQSKQ-UHFFFAOYSA-N fenoxycarb Chemical compound C1=CC(OCCNC(=O)OCC)=CC=C1OC1=CC=CC=C1 HJUFTIJOISQSKQ-UHFFFAOYSA-N 0.000 description 1
229940013764 fipronil Drugs 0.000 description 1
229940013317 fish oils Drugs 0.000 description 1
RYLHNOVXKPXDIP-UHFFFAOYSA-N flufenoxuron Chemical compound C=1C=C(NC(=O)NC(=O)C=2C(=CC=CC=2F)F)C(F)=CC=1OC1=CC=C(C(F)(F)F)C=C1Cl RYLHNOVXKPXDIP-UHFFFAOYSA-N 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
235000019256 formaldehyde Nutrition 0.000 description 1
239000013505 freshwater Substances 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
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238000010438 heat treatment Methods 0.000 description 1
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000005842 heteroatom Chemical group 0.000 description 1
RGNPBRKPHBKNKX-UHFFFAOYSA-N hexaflumuron Chemical compound C1=C(Cl)C(OC(F)(F)C(F)F)=C(Cl)C=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F RGNPBRKPHBKNKX-UHFFFAOYSA-N 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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238000006460 hydrolysis reaction Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
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239000002655 kraft paper Substances 0.000 description 1
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OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
230000007774 longterm Effects 0.000 description 1
229960000521 lufenuron Drugs 0.000 description 1
PWPJGUXAGUPAHP-UHFFFAOYSA-N lufenuron Chemical compound C1=C(Cl)C(OC(F)(F)C(C(F)(F)F)F)=CC(Cl)=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F PWPJGUXAGUPAHP-UHFFFAOYSA-N 0.000 description 1
150000002736 metal compounds Chemical class 0.000 description 1
229910044991 metal oxide Inorganic materials 0.000 description 1
150000004706 metal oxides Chemical class 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
239000004530 micro-emulsion Substances 0.000 description 1
150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
ZWRDBWDXRLPESY-UHFFFAOYSA-N n-benzyl-n-ethylethanamine Chemical class CCN(CC)CC1=CC=CC=C1 ZWRDBWDXRLPESY-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
229920001220 nitrocellulos Polymers 0.000 description 1
125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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239000004006 olive oil Substances 0.000 description 1
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229940006093 opthalmologic coloring agent diagnostic Drugs 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
AZHVQJLDOFKHPZ-UHFFFAOYSA-N oxathiazine Chemical class O1SN=CC=C1 AZHVQJLDOFKHPZ-UHFFFAOYSA-N 0.000 description 1
239000006174 pH buffer Substances 0.000 description 1
IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
239000000123 paper Substances 0.000 description 1
230000000149 penetrating effect Effects 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
229960000490 permethrin Drugs 0.000 description 1
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239000003209 petroleum derivative Substances 0.000 description 1
JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical compound C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 1
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WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
239000000049 pigment Substances 0.000 description 1
239000001839 pinus sylvestris Substances 0.000 description 1
239000011120 plywood Substances 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
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239000004300 potassium benzoate Substances 0.000 description 1
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238000004321 preservation Methods 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
229940032159 propylene carbonate Drugs 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
125000003373 pyrazinyl group Chemical group 0.000 description 1
125000002098 pyridazinyl group Chemical group 0.000 description 1
125000000714 pyrimidinyl group Chemical group 0.000 description 1
125000005493 quinolyl group Chemical group 0.000 description 1
239000002516 radical scavenger Substances 0.000 description 1
238000009877 rendering Methods 0.000 description 1
239000000523 sample Substances 0.000 description 1
235000003441 saturated fatty acids Nutrition 0.000 description 1
239000012047 saturated solution Substances 0.000 description 1
HPYNBECUCCGGPA-UHFFFAOYSA-N silafluofen Chemical compound C1=CC(OCC)=CC=C1[Si](C)(C)CCCC1=CC=C(F)C(OC=2C=CC=CC=2)=C1 HPYNBECUCCGGPA-UHFFFAOYSA-N 0.000 description 1
238000004513 sizing Methods 0.000 description 1
239000000344 soap Substances 0.000 description 1
235000002639 sodium chloride Nutrition 0.000 description 1
229960004025 sodium salicylate Drugs 0.000 description 1
KVCGISUBCHHTDD-UHFFFAOYSA-M sodium;4-methylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1 KVCGISUBCHHTDD-UHFFFAOYSA-M 0.000 description 1
241000894007 species Species 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000003432 sterols Chemical class 0.000 description 1
235000003702 sterols Nutrition 0.000 description 1
229920005792 styrene-acrylic resin Polymers 0.000 description 1
NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical class NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
125000003375 sulfoxide group Chemical group 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
239000002424 termiticide Substances 0.000 description 1
150000003505 terpenes Chemical class 0.000 description 1
235000007586 terpenes Nutrition 0.000 description 1
ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
229960005199 tetramethrin Drugs 0.000 description 1
150000003536 tetrazoles Chemical class 0.000 description 1
239000004753 textile Substances 0.000 description 1
NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 description 1
150000003573 thiols Chemical group 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
239000001993 wax Substances 0.000 description 1
239000003171 wood protecting agent Substances 0.000 description 1
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150000003751 zinc Chemical class 0.000 description 1
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Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
- B27K3/34—Organic impregnating agents
- B27K3/343—Heterocyclic compounds
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
- B27K3/52—Impregnating agents containing mixtures of inorganic and organic compounds
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
- B27K3/34—Organic impregnating agents
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
- B27K3/34—Organic impregnating agents
- B27K3/50—Mixtures of different organic impregnating agents
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31971—Of carbohydrate
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31971—Of carbohydrate
- Y10T428/31975—Of cellulosic next to another carbohydrate
- Y10T428/31978—Cellulosic next to another cellulosic
- Y10T428/31986—Regenerated or modified
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31971—Of carbohydrate
- Y10T428/31989—Of wood

Landscapes

Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Wood Science & Technology (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Plant Pathology (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Dentistry (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Forests & Forestry (AREA)
Chemical & Material Sciences (AREA)
Inorganic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Chemical And Physical Treatments For Wood And The Like (AREA)
Dispersion Chemistry (AREA)
Toxicology (AREA)

CA 2722770 2008-04-30 2009-04-30 Antisapstain compositions comprising a haloalkynyl compound, an azole and an unsaturated acid Expired - Fee Related CA2722770C (en)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
GB0807905A GB2459691B (en)	2008-04-30	2008-04-30	Formulations
GB0807905.5		2008-04-30
PCT/GB2009/001104 WO2009133374A2 (en)	2008-04-30	2009-04-30	Antisapstain compositions comprising a haloalkynyl compound, an azole and an unsaturated acid

Publications (2)

Publication Number	Publication Date
CA2722770A1 CA2722770A1 (en)	2009-11-05
CA2722770C true CA2722770C (en)	2015-02-17

Family

ID=39522845

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA 2722770 Expired - Fee Related CA2722770C (en)	2008-04-30	2009-04-30	Antisapstain compositions comprising a haloalkynyl compound, an azole and an unsaturated acid

Country Status (13)

Country	Link
US (1)	US8435643B2 (pt)
EP (1)	EP2282637B1 (pt)
JP (2)	JP5906084B2 (pt)
KR (2)	KR20110013407A (pt)
CN (1)	CN102202510B (pt)
AU (1)	AU2009241641B2 (pt)
BR (1)	BRPI0911776A2 (pt)
CA (1)	CA2722770C (pt)
GB (1)	GB2459691B (pt)
MX (1)	MX2010011577A (pt)
NZ (2)	NZ588690A (pt)
RU (1)	RU2489252C2 (pt)
WO (1)	WO2009133374A2 (pt)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US9539795B2 (en)	2008-08-07	2017-01-10	Ashland Licensing And Intellectual Property Llc	Matte substrate
CN102595887A (zh) *	2009-10-08	2012-07-18	泰卡聚合物公司	抗微生物组合物
GB2479556A (en) *	2010-04-13	2011-10-19	Arch Timber Protection Ltd	Wood preservative formulation
FR2973270B1 (fr) *	2011-03-28	2013-03-29	A R C Nucleart	Traitement oleothermique permettant de stabiliser dimensionnellement le bois
US10433548B2 (en) *	2012-10-12	2019-10-08	Arch Chemicals, Inc.	Biocidal compositions comprising iron chelators
US9468210B2 (en) *	2013-06-18	2016-10-18	Syngenta Participations Ag	Compositions for post-harvest treatment and related methods
JP2015003863A (ja) *	2013-06-19	2015-01-08	住化エンバイロメンタルサイエンス株式会社	木材用抗菌組成物
JP5531269B1 (ja) *	2013-07-19	2014-06-25	株式会社片山化学工業研究所	鉄の防食方法及び木材処理方法
EP3071038B1 (en)	2013-11-19	2021-12-15	Arch Chemicals, Inc.	Enhanced preservative
CA2852530A1 (en)	2014-05-21	2015-11-21	The Sansin Corporation	Antimicrobial composition for protecting wood
JP7305188B2 (ja) *	2015-07-30	2023-07-10	住化エンバイロメンタルサイエンス株式会社	木材用抗菌組成物
US9717246B1 (en) *	2016-05-24	2017-08-01	Kop-Coat, Inc.	Method and related solution for protecting wood through enhanced penetration of wood preservatives employing buffered amine oxides and alkoxylated oils
WO2019064283A1 (en)	2017-09-29	2019-04-04	0903608 B.C. Ltd.	SYNERGISTIC PESTICIDAL COMPOSITIONS AND METHODS OF DELIVERY OF ACTIVE AGENTS
CA3114046C (en)	2018-09-27	2022-07-19	0903608 B.C. Ltd.	Synergistic pesticidal compositions and methods for delivery of insecticidal active ingredients
WO2020061706A1 (en) *	2018-09-27	2020-04-02	0903608 B.C. Ltd.	Synergistic pesticidal compositions and methods for delivery of active ingredients
WO2021172390A1 (ja) *	2020-02-27	2021-09-02	日本曹達株式会社	殺菌剤組成物
JP2020090546A (ja) *	2020-03-03	2020-06-11	住化エンバイロメンタルサイエンス株式会社	木材用抗菌組成物

Family Cites Families (39)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3923870A (en)	1973-07-11	1975-12-02	Troy Chemical Corp	Urethanes of 1-halogen substituted alkynes
US4259350A (en)	1978-03-15	1981-03-31	Sankyo Company Limited	Iodopropargyl derivatives, their use and preparation
IL75979A (en)	1984-08-10	1988-10-31	Mitsui Toatsu Chemicals	Propargyloxyacetonitrile derivatives,their preparation and fungicidal and herbicidal compositions containing them
US4616004A (en)	1984-09-27	1986-10-07	Chevron Research Company	1-iodopropargyl-3,4-disubstituted-Δ2 -1,2,4-triazolidin-5-one fungicides
DE3510203A1 (de)	1985-03-21	1986-09-25	Bayer Ag, 5090 Leverkusen	Neue iodpropargylether, ein verfahren zu ihrer herstellung und ihre verwendung
US4945109A (en)	1988-08-24	1990-07-31	Buckman Laboratories International, Inc.	Ester of carbamic acid useful as a microbicide and a preservative
SU1659194A1 (ru) *	1988-10-28	1991-06-30	Сенежская Лаборатория Консервирования Древесины Всесоюзного Научно-Исследовательского Института Деревообрабатывающей Промышленности	Средство дл защиты древесины от синевы и плесени
GB8908794D0 (en) *	1989-04-19	1989-06-07	Janssen Pharmaceutica Nv	Synergistic compositions containing propiconazole and tebuconazole
US5059629A (en) *	1990-02-16	1991-10-22	The Dow Chemical Company	Biocidal foams
US5196407A (en) *	1990-05-23	1993-03-23	Desowag Materialschutz Gmbh	Composition for preserving wood and wood materials
DE4016602A1 (de) *	1990-05-23	1991-11-28	Desowag Materialschutz Gmbh	Mittel zum konservieren von holz und holzwerkstoffen
US5399190A (en)	1990-09-03	1995-03-21	Shell South Africa (Pty.) Ltd.	Wood preservatives
DE4113158A1 (de)	1991-04-23	1992-10-29	Bayer Ag	Mikrobizide wirkstoffkombinationen
DE4122867A1 (de) *	1991-07-11	1993-01-14	Bayer Ag	Mikrobizide wirkstoffkombinationen
DE4441672A1 (de)	1994-11-23	1996-05-30	Basf Ag	Holzschutzmittel
JP3159424B2 (ja) *	1995-01-12	2001-04-23	北興化学工業株式会社	工業用防腐防かび剤
JP3604532B2 (ja) *	1997-05-15	2004-12-22	北興化学工業株式会社	防腐防かび剤
JPH1121205A (ja) *	1997-07-03	1999-01-26	Mitsui Chem Inc	塩化ビニル樹脂成形用組成物
JP4066209B2 (ja) *	1998-03-23	2008-03-26	住化エンビロサイエンス株式会社	工業用防腐防カビ組成物
JPH11302114A (ja) *	1998-04-21	1999-11-02	Mitsui Chem Inc	防菌防カビ剤
FR2784115B1 (fr) *	1998-10-05	2000-12-15	Rhodia Chimie Sa	Composition de revetements contenant des silicones fonctionnalisees
DE19947182A1 (de) *	1999-09-30	2001-05-03	Wacker Chemie Gmbh	Holzschutzmittel, Verfahren zu ihrer Herstellung und ihre Verwendung
CA2439640A1 (en) *	2001-03-01	2002-09-12	Lonza Inc.	Combination of an iodopropynyl derivative with a ketone acid or its salt and/or with an aromatic carboxylic acid or its salt
JP2003267806A (ja) *	2002-03-14	2003-09-25	Taisho Technos Co Ltd	工業用抗菌防かび剤
CN100351475C (zh) *	2002-06-07	2007-11-28	密克罗伴产品公司	抗微生物墙板
US7056919B2 (en) *	2003-01-24	2006-06-06	Kopcoat, Inc.	Synergistic combination of fungicides to protect wood and wood-based products and wood treated by such combination as well as methods of making the same
BRPI0411340B1 (pt) *	2003-06-17	2013-04-09		composiÇço conservante de madeira, mÉtodo para produzir a mesma e madeira impregnada com este mÉtodo.
JP2005047056A (ja) *	2003-07-30	2005-02-24	Shinto Fine Co Ltd	木材防腐組成物、木材防腐保存方法及び防腐処理木材
RU2346996C2 (ru)	2004-06-29	2009-02-20	ЮРОПИЭН НИКЕЛЬ ПиЭлСи	Усовершенствованное выщелачивание основных металлов
US8486915B2 (en) *	2004-08-12	2013-07-16	Isp Investments Inc.	Compositions of water-insoluble active organic compounds
FI118002B (fi)	2005-01-04	2007-05-31	Granula Ab Ltd Oy	Menetelmä aineen imeyttämiseksi puuhun
DE102005022148A1 (de) *	2005-05-13	2006-11-23	Lanxess Deutschland Gmbh	Fungizide Mischungen
US7655281B2 (en) *	2005-05-24	2010-02-02	Kop-Coat, Inc.	Method of protecting wood through enhanced penetration of wood preservatives and related solution
EP1895898B1 (en)	2005-06-29	2011-02-16	Compumedics Limited	Sensor assembly with conductive bridge
DE602006010580D1 (de)	2005-09-01	2009-12-31	Janssen Pharmaceutica Nv	Verwendung alkoxylierter amine zur erhöhung der wasserabweisung von holz
WO2007092580A2 (en) *	2006-02-08	2007-08-16	Phibro-Tech Inc.	Biocidal azole emulsion concentrates having high active ingredient content
WO2007109735A2 (en) *	2006-03-22	2007-09-27	Mississippi State University	A nonleachable composition and method to use
GB2438404A (en) *	2006-05-24	2007-11-28	Arch Timber Protection Ltd	Preserving wood with an amine oxide, an azole and a specified amine or quaternary ammonium compound, in synergistic proportions
JP4993448B2 (ja) *	2006-09-28	2012-08-08	日本エンバイロケミカルズ株式会社	木材保存剤

2008
- 2008-04-30 GB GB0807905A patent/GB2459691B/en not_active Expired - Fee Related
2009
- 2009-04-30 CA CA 2722770 patent/CA2722770C/en not_active Expired - Fee Related
- 2009-04-30 KR KR1020107025734A patent/KR20110013407A/ko not_active Ceased
- 2009-04-30 NZ NZ58869009A patent/NZ588690A/xx not_active IP Right Cessation
- 2009-04-30 CN CN200980115919.2A patent/CN102202510B/zh not_active Expired - Fee Related
- 2009-04-30 KR KR1020167011172A patent/KR20160054029A/ko not_active Withdrawn
- 2009-04-30 AU AU2009241641A patent/AU2009241641B2/en not_active Ceased
- 2009-04-30 EP EP09738404.4A patent/EP2282637B1/en not_active Not-in-force
- 2009-04-30 RU RU2010147324/13A patent/RU2489252C2/ru not_active IP Right Cessation
- 2009-04-30 NZ NZ60299309A patent/NZ602993A/en not_active IP Right Cessation
- 2009-04-30 BR BRPI0911776-8A patent/BRPI0911776A2/pt not_active Application Discontinuation
- 2009-04-30 JP JP2011506771A patent/JP5906084B2/ja not_active Expired - Fee Related
- 2009-04-30 MX MX2010011577A patent/MX2010011577A/es active IP Right Grant
- 2009-04-30 WO PCT/GB2009/001104 patent/WO2009133374A2/en not_active Ceased
2010
- 2010-10-28 US US12/925,730 patent/US8435643B2/en not_active Expired - Fee Related
2015
- 2015-10-26 JP JP2015209749A patent/JP2016094400A/ja active Pending

Also Published As

Publication number	Publication date
EP2282637B1 (en)	2015-06-17
WO2009133374A2 (en)	2009-11-05
AU2009241641B2 (en)	2014-03-13
GB2459691B (en)	2013-05-22
WO2009133374A3 (en)	2011-06-23
US20110111245A1 (en)	2011-05-12
AU2009241641A1 (en)	2009-11-05
JP2016094400A (ja)	2016-05-26
GB0807905D0 (en)	2008-06-04
NZ602993A (en)	2014-05-30
CN102202510B (zh)	2015-05-20
US8435643B2 (en)	2013-05-07
KR20110013407A (ko)	2011-02-09
MX2010011577A (es)	2011-05-30
GB2459691A (en)	2009-11-04
JP2011522786A (ja)	2011-08-04
CA2722770A1 (en)	2009-11-05
BRPI0911776A2 (pt)	2015-08-04
NZ588690A (en)	2012-11-30
JP5906084B2 (ja)	2016-04-20
KR20160054029A (ko)	2016-05-13
EP2282637A2 (en)	2011-02-16
RU2489252C2 (ru)	2013-08-10
CN102202510A (zh)	2011-09-28
RU2010147324A (ru)	2012-06-10

Legal Events

Date	Code	Title	Description
2012-05-29	EEER	Examination request
2019-06-11	MKLA	Lapsed	Effective date: 20190430

Publication	Publication Date	Title
AU2009241641B2 (en)	2014-03-13	Antisapstain compositions comprising a haloalkynyl compound, an azole and an unsaturated acid
CA2796022C (en)	2020-04-28	Wood preservative formulations comprising isothiazolones which provide protection against surface staining
AU2007253048B2 (en)	2013-03-21	Wood preservative formulations
CN107683192A (zh)	2018-02-09	抗真菌增效剂
DE4016602A1 (de)	1991-11-28	Mittel zum konservieren von holz und holzwerkstoffen
CN107206618A (zh)	2017-09-26	木材防腐剂制剂
AU2014200779B2 (en)	2015-07-09	Antisapstain compositions comprising a haloalkynyl compound, an azole and an unsaturated acid
AU2013200225B9 (en)	2014-11-13	Wood preservative formulations